تفاعل #1511328

ord-ddfbcb6be3ba40e1ab79d9661c376352

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe residue was purified through an SCX cartridge
  2. 2
    غسيلeluting with 0-60% MeCN in water

الإجراء التجريبي

The title compound was prepared according to Method 1 using (S)-3-(tert-butoxycarbonyl)-2,2-dimethyloxazolidine-4-carboxylic acid and 3′,4′-diaminobiphenyl-4-carbonitrile (Preparation 82). The residue was purified through an SCX cartridge followed by reverse phase column chromatography eluting with 0-60% MeCN in water.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08927587B2uspto-grants-2015_01